FDA UDI In Commercial Distribution 🇺🇸 United States

7LS

DI: 00031262096531 · Model: FA7-1400J · FKA DISTRIBUTING CO., LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
7LS
Primary DI
00031262096531
Version / Model
FA7-1400J
Catalog Number
FA7-1400J
Company Name
FKA DISTRIBUTING CO., LLC
Labeler DUNS
183280973
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-02-29
Public Version
1
Public Version Date
2020-03-09
Public Version Status
New
Public Device Record Key
5af25514-d370-4e2d-9ba7-fab8755a3109

Device Description

ReSculpt Micro-Current & Light Therapy

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
NFO Stimulator, Transcutaneous Electrical, Aesthetic Purposes

GMDN Terms

Code Name
35372 Analgesic transcutaneous electrical nerve stimulation system

Identifiers

Type ID
Primary 00031262096531

Customer Contacts

Phone
248-863-3176

Premarket Submissions

Submission Number Supplement Number
K162106 000